Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262902Generated: October 30, 2026

Dimethyl Sulfoxide → N-1,2-benzisoxazol-3-yl-4-(4-phenyl-1,3-oxazol-2-yl)piperazine-1-carboxamide

https://huagongshe.com/reaction/2262902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(4-Phenyl-1,3-oxazol-2-yl)piperazineHCID 68775735—
ReactantBis(2,2,2-trichloroethyl) 1,2-benzisoxazol-3-ylimidodicarbonateHCID 86625471—
SolventWaterHCID 962—
ProductN-1,2-benzisoxazol-3-yl-4-(4-phenyl-1,3-oxazol-2-yl)piperazine-1-carboxamideHCID 68777876—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 1-(4-Phenyl-1,3-oxazol-2-yl)piperazine (391 mg, 0.807 mmol), bis(2,2,2-trichloroethyl) 1,2-benzisoxazol-3-ylimidodicarbonate (370 mg, 1.61 mmol), diisopropylethylamine (0.141 ml, 0.807 mmol) and dimethylsulfoxide (5 ml) was stirred at 70° C. for 2 hours. The reaction mixture was poured to water and extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=2:1) to give the desired product as a solid. The resulting solid was recrystallized from a mixed solvent of ethyl acetate and hexane to give 44.0 mg (14.1%) of the desired product. mp 171-172° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851473B2
Source datasetuspto-grants-2010_12
ORD IDord-9ae19a1ebc874e4193a4b0ba44e69f4c
Source noteuspto-grants-2010_12